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Clinical Trials/NCT03778827
NCT03778827
Active, not recruiting
Not Applicable

A Center Based Randomized Controlled Trial of Pivotal Response Treatment for Preschoolers With Autism

Stanford University1 site in 1 country75 target enrollmentMay 13, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Autism Spectrum Disorder
Sponsor
Stanford University
Enrollment
75
Locations
1
Primary Endpoint
Mean change from baseline on the Brief Observation of Communication Change (BOSCC) total score at 12 Weeks
Status
Active, not recruiting
Last Updated
5 months ago

Overview

Brief Summary

The purpose of this study is to examine the effectiveness of pivotal response training (PRT) in an intensive center-based environment to treat social communication deficits in children with autism spectrum disorder (ASD).

Detailed Description

The purpose of this study is to examine the effectiveness of pivotal response training (PRT) in an intensive center-based preschool environment to treat social communication deficits in children with autism spectrum disorder (ASD). The study will compare Pivotal Response Treatment (PRT) to a delayed treatment group (DTG). PRT is a naturalistic behavioral intervention based on the principles of applied behavior analysis which has shown to be effective in treating the core deficits in children with ASD. The study will compare the combination of parent training with intensive center-based PRT (PRT-C) to a DTG and will include 44 children ages 2 to 3.11 years with ASD and social communication deficits.

Registry
clinicaltrials.gov
Start Date
May 13, 2019
End Date
June 1, 2026
Last Updated
5 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Antonio Hardan

Professor of Psychiatry and Behavioral Sciences

Stanford University

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of Autism Spectrum Disorder (ASD) based on clinical interview and Diagnostic and Statistical Manual, 5th edition (DSM-5) and confirmed using the Autism Diagnostic Interview Revised (ADI-R) and Autism Diagnostic Observation Schedule, 2nd edition (ADOS-2) or Childhood Autism Rating Scale (CARS-2); Diagnostic and Statistical Manual, 5th edition (DSM-5), and expert clinical opinion
  • Boys and girls between 2 years and 3 years and 11 months
  • Ability to participate in the testing procedures to the extent that valid standard scores can be obtained
  • Stable treatment (e.g., applied behavior analysis (ABA), speech therapy, psychotropic medication(s) or biomedical intervention(s) for at least 1 month prior to baseline measurements with no anticipated changes during study participation
  • Developmentally delayed with Mullen Scales of Early Learning (MSEL) or Developmental Profile (DP-4) composite score below 85 (1 Standard Deviation below the mean)
  • Availability of at least one English-speaking parent who can consistently participate in parent training and research measures.

Exclusion Criteria

  • Current or lifetime diagnosis of severe psychiatric disorder (e.g., bipolar disorder, etc.)
  • Presence of active medical problem (e.g., unstable seizure disorder or heart disease)
  • Child primary language other than English
  • Previous adequate trial of Pivotal Response Treatment
  • More than 15 hours per week of in-home applied behavior analysis (ABA).

Outcomes

Primary Outcomes

Mean change from baseline on the Brief Observation of Communication Change (BOSCC) total score at 12 Weeks

Time Frame: Baseline and Week 12

Mean change from baseline on the frequency if the child's functional utterances on the structured lab observation at 12 Weeks

Time Frame: Baseline and Week 12

Mean Change from baseline on the Social Responsiveness Scale-2 Total Score at 12 Weeks

Time Frame: Baseline and Week 12

Secondary Outcomes

  • Mean change from baseline on the Vineland Adaptive Behavior Scales 3rd Edition Socialization subscale at 12 Weeks(Baseline and Week 12)
  • Mean change from baseline on the MacArthur-Bates Communication Development Inventory at 12 Weeks(Baseline and Week 12)

Study Sites (1)

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